Deprotonation of the Transition Metal Hydride (η5-C5Me5)(PMe3)IrH2. Synthesis and Chemistry of the Strongly Basic Lithium Iridate (η5-C5Me5)(PMe3)Ir(H)(Li)-Reference-Cited by-同舟云学术

Deprotonation of the Transition Metal Hydride (η5-C5Me5)(PMe3)IrH2. Synthesis and Chemistry of the Strongly Basic Lithium Iridate (η5-C5Me5)(PMe3)Ir(H)(Li)

Published:1999-04-25 Issue:10 Volume:18 Page:2005-2020
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Peterson Thomas H.¹,Golden Jeffery T.¹,Bergman Robert G.¹

Affiliation:

1. Department of Chemistry, University of California, Berkeley, California 94720

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om980945d

Reference88 articles.

1. Heterometallic Dinuclear Complexes by Ethene Displacement with Grignard Compounds or Diorganomagnesium Compounds

2. Synthesis of trimethylphosphine-substituted (pentamethylcyclopentadienyl)iridium hydride complexes; protonation and deprotonation of (pentamethylcyclopentadienyl)(trimethylphosphine)iridium dihydride

3. Preparation and reactions of cyclo-tetra-µ-lithio-tetrakis[bis(η-cyclo-pentadienyl)hydrido-molybdenum] and -tungsten] and some bis(η-cyclopentadienyl) derivatives of molybdenum and tungsten

4. Deprotonation and anionic rearrangements of organometallic compounds. Reactions of the hydride complex (η5-C5H5)Re(NO)(PPh3)(H) with n-butyl-lithium–tetramethylethylenediamine

5. Reactivity of zero-valent metalloporphyrin dianions toward organic electrophiles

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